Ni Electrocatalysts for the Oxygen Evolution Reaction in Acidic Electrolyte"/>

This study introduces a sustainable microwave-assisted polyol method for rapidly synthesizing IrNi catalysts with enhanced oxygen evolution activity. The strong synergy between Ir and Ni delivers higher intrinsic performance than commercial IrO₂, offering a promising alternative to conventional synthesis routes.

This study investigates a microwave-assisted synthesis method for producing IrNi bimetallic catalysts for the oxygen evolution reaction in acidic environment. Due to the high cost of iridium-based catalysts used in the anodes of proton-exchange membrane electrolyzers, reducing the noble metal content while maintaining high performance is crucial. In this work, materials with various IrNi atomic ratios are synthesized and their impact on the catalyst microstructure, phase composition, and electrochemical performance is evaluated. The results reveal a synergistic effect between the two metals, with 60 at% Ni identified as the optimal nominal composition. This catalyst achieves an overpotential of 274 mV at 10 mA cm⁻² and a Tafel slope of 49 mV dec⁻¹ in 0.5 M H₂SO₄ electrolyte, outperforming commercial IrO₂ (320 mV at 10 mA cm⁻² and 56 mV dec⁻¹). The higher activity is retained after both a 6 h chronoamperometry and an accelerated degradation test, during which Ni acts as a sacrificial component and the electrochemically surface area of the films increases. Overall, this study demonstrates the potential of microwave-assisted synthesis, a greener and faster alternative to conventional methods, for developing low Ir-content catalysts with enhanced performance.